F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
Disease: Primary Raynaud Phenomenon ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0151445
Disease: Primary Raynaud Phenomenon
Primary Raynaud Phenomenon 		0.010 GeneticVariation disease BEFREE FVLeiden, prothrombin G20210A, and polymorphism, prothrombin G20210A mutations have no apparent effect on the etiology of primary Raynaud's phenomenon. 21157301 2011